Canonical Allele Identifier: CA511291711

Gene: MIR646HG

Linked Data

• gnomAD v4: 20-60320912-A-G
• MyVariant Identifiers: chr20:g.58895970A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320912A>G , CM000682.2:g.60320912A>G	GRCh38
NC_000020.10:g.58895970A>G , CM000682.1:g.58895970A>G	GRCh37
NC_000020.9:g.58329365A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.699A>G